Evidence map›Paper›PMID 31622411›Full record

ArticlePloS one2019

The FTO genetic variants are associated with dietary intake and body mass index amongst Emirati population.

Maha Saber-Ayad, Shaista Manzoor, Hadia Radwan, Sarah Hammoudeh, Rahaf Wardeh, Ahmed Ashraf, Hussein Jabbar, Rifat Hamoudi

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed, 1 pooled it
2.1field-weighted citation impact, top 12% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

13 citing papers in PubMed, 1 synthesis or guideline pooled it, 23 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors at 2 institutions in 2 countries.

Maha Saber-AyadCollege of Medicine, University of Sharjah, Sharjah, UAE.ORCID 0000-0002-9287-7621
Shaista ManzoorCollege of Medicine, University of Sharjah, Sharjah, UAE.
Hadia RadwanCollege of Medicine, University of Sharjah, Sharjah, UAE.ORCID 0000-0002-3930-2554
Sarah HammoudehCollege of Medicine, University of Sharjah, Sharjah, UAE.
Rahaf WardehCollege of Medicine, University of Sharjah, Sharjah, UAE.
Ahmed AshrafCollege of Medicine, University of Sharjah, Sharjah, UAE.
Hussein JabbarCollege of Medicine, University of Sharjah, Sharjah, UAE.
Rifat HamoudiCollege of Medicine, University of Sharjah, Sharjah, UAE.
University of Sharjah · AECairo University · EG

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe risk of obesity is determined by complex interactions between genetic and environmental factors. Little research to date has investigated the interaction between gene and food intake. The aim of the current study is to explore the potential effect of fat mass and obesity-associated protein gene (FTO) rs9939609 and rs9930506 single nucleotide polymorphism (SNP) on the pattern of food intake in the Emirati population.

methodsAdult healthy Emirati subjects with Body mass index (BMI) of 16-40 kg/m2 were included in the study. Genotyping for FTO rs9939609(A>T) and rs9930506(A>G) was performed using DNA from saliva samples. Subjects were categorized according to the WHO classification by calculating the BMI to compare different classes. Dietary intake was assessed by a sixty-one-item FFQ that estimated food and beverage intakes over the past year. The daily energy, macronutrient, and micronutrient consumption were computed.

resultsWe included 169 subjects in the final analysis (mean age 30.49± 9.1years, 57.4% females). The mean BMI of the study population was 26.19 kg/m2. Both SNPs were in Hardy Weinberg Equilibrium. The rs9939609 AA genotype was significantly associated with higher BMI (p = 0.004); the effect was significant in females (p = 0.028), but not in males (p = 0.184). Carbohydrate intake was significantly higher in AA subjects with a trend of lower fat intake compared to other genotypes. The odds ratio for the AA was 3.78 in the fourth quartile and 2.67 for the A/T in the second quartile of total carbohydrate intake, considering the first quartile as a reference (95% CI = 1.017-14.1 and 1.03-6.88, respectively). Fat intake was significantly lower in the FTO rs9930506 GG subjects. The presence of FTO rs9930506 GG genotype decreased the fat intake in subjects with FTO rs9939609 AA (p = 0.037).

conclusionsThe results of this study highlight the interaction of the FTO risk alleles on the food intake in Emirati subjects. The FTO rs9939609 AA subjects had higher carbohydrate and lower fat intake. The latter was accentuated in presence of rs9930506 GG genotype.

Indexed as

AdolescentAdultAllelesAlpha-Ketoglutarate-Dependent Dioxygenase FTOBody Mass IndexDietary CarbohydratesFemaleGene FrequencyGenotypeHumansMaleMiddle AgedObesityPolymorphism, Single NucleotideYoung AdultAlpha-Ketoglutarate-Dependent Dioxygenase FTODietary CarbohydratesFTO protein, human

Identifiers

PMID31622411
PMCPMC6797190
OpenAlexW2981170008

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.